FDA inspection

Criticare Technologies, Inc.: FDA inspection ending Oct 29, 2019

FDA inspection 1107892 · Voluntary Action Indicated (VAI) · Warwick, RI

Key facts

Inspection ID 1107892
Firm Criticare Technologies, Inc.
FEI number 3012238587
Address 125 Commerce Park Rd
City Warwick
State RI
ZIP 02886
Country United States
Fiscal year 2020
Inspection end date Oct 29, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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